Hereditary elliptocytosis due to alpha spectrin defect

disorder

SNOMED 8857001CUI C0272040

Overview

Hereditary elliptocytosis due to alpha spectrin defect is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary ovalocytosis(parent)

Quick Facts

SNOMED CT: 8857001
UMLS CUI: C0272040
Fully Specified Name: Hereditary elliptocytosis due to alpha spectrin defect (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.